NDC 54868-4817
Paroxetine 40 mg tablet, film coated
On the label: Physicians Total Care, Inc.. It's repackaged: Physicians Total Care, Inc. rebottles it from Apotex Corp.'s NDC 60505-0101.
Where the pills inside were made
This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Apotex Corp. names for other drugs.
Repackaging site
- Physicians Total Care, Inc., Tulsa, Oklahoma, United States · repackages it and relabels it
Recalls
- Nov 1, 2023 · Class II · Apotex Corp.
Failed Impurities/Degradation Specifications-Out of specification (OOS) results for the excipient Amadori Glucose adduct of Paroxetine
Lots: Lot numbers: RV0131, RV2387, RV2389, RW3296, RV2388; Exp. 08/2024
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Paroxetine: every company that makes it
- Form
- tablet, film coated
- Strength
- 40 mg
- Approval
- ANDA ANDA075356
- On the market since
- Feb 18, 2009
- Package NDCs
54868-4817-054868-4817-154868-4817-2- Official label
- DailyMed (National Library of Medicine), updated Sep 10, 2012
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?